Canonical Allele Identifier: CA389009220
Gene: MYH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392968C>A , CM000676.2:g.23392968C>A GRCh38
NC_000014.8:g.23862177C>A , CM000676.1:g.23862177C>A GRCh37
NC_000014.7:g.22932017C>A NCBI36
NG_023444.1:g.20310G>T , LRG_389:g.20310G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.3195G>T MANE Select ENSP00000386041.3:p.Gln1065His
ENST00000356287.3:c.3195G>T ENSP00000348634.3:p.Gln1065His
ENST00000405093.7:c.3195G>T ENSP00000386041.3:p.Gln1065His
NM_002471.3:c.3195G>T , LRG_389t1:c.3195G>T NP_002462.2:p.Gln1065His
NM_002471.4:c.3195G>T MANE Select NP_002462.2:p.Gln1065His